Early real-world effectiveness of ustekinumab for Crohn's disease

被引:30
|
作者
Harris, Richard James [1 ]
McDonnell, Martin [1 ]
Young, David [1 ]
Bettey, Marion [1 ]
Downey, Louise [1 ]
Pigott, Lucinda [1 ]
Felwick, Richard [1 ]
Gwiggner, Markus [1 ]
Cummings, J. R. Fraser [1 ,2 ]
机构
[1] Univ Hosp Southampton NHS Fdn Trust, Dept Gastroenterol, Southampton, Hants, England
[2] Univ Southampton, Fac Med, Southampton, Hants, England
关键词
INDUCTION; THERAPY; MAINTENANCE; EXPERIENCE; MANAGEMENT; SAFETY;
D O I
10.1136/flgastro-2019-101237
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective To understand the effectiveness of ustekinumab in treating Crohn's disease (CD) in a UK real-world setting. Design Retrospective cohort study using prospectively maintained clinical records. Setting Single UK inflammatory bowel disease centre. Patients Adult patients with an established diagnosis of CD prescribed ustekinumab outside of clinical trials at University Hospital Southampton (UHS). Interventions Ustekinumab, a monoclonal antibody to the shared p40 subunit of interleukin (IL) 12 and IL-23 as part of routine clinical care. Main outcome measures Effectiveness as measured by an improvement in physician's global assessment, drug persistence and improvement in biomarkers (C-reactive protein (CRP), albumin and calprotectin). Results 84 patients were included, 72 had a postinduction review and 49 had 1-year data. At postinduction clinical review, clinical response occurred in 53% of patients and clinical remission occurred in 8%. For patients on ustekinumab at 1 year, clinical response occurred in 71% and remission in 14%. Adverse events included four patients with infections requiring admission, one drug-related rash, five CD surgeries and two CD exacerbations. Conclusions Ustekinumab was well tolerated in a complex UK CD population and demonstrated benefit to patients in terms of clinical response and improvement of biomarkers and with some patients attaining clinical remission. No unexpected safety signals were seen.
引用
收藏
页码:111 / 116
页数:6
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